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423734

Sigma-Aldrich

6-Methyl-1-indanone

99%

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About This Item

Empirical Formula (Hill Notation):
C10H10O
CAS Number:
Molecular Weight:
146.19
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

bp

70 °C/0.4 mmHg (lit.)

mp

60-62 °C (lit.)

SMILES string

Cc1ccc2CCC(=O)c2c1

InChI

1S/C10H10O/c1-7-2-3-8-4-5-10(11)9(8)6-7/h2-3,6H,4-5H2,1H3

InChI key

DBOXRDYLMJMQBB-UHFFFAOYSA-N

General description

6-Methyl-1-indanone is a substituted indanone. It has been synthesized in high quantum yields by the photolysis of α-chloro-2′,5′-dimethylacetophenone. It is formed as one of the photoproduct during the irradiation of 2,5-dimethylphenacyl (DMP) esters. It is reported to be one of the semivolatile component of lamina cigarette smoke.

Application

6-Methyl-1-indanone was used as a starting material for the synthesis of branched alkyl indanes (BINs).

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

423734-1G:
423734-5G:
423734-VAR:
423734-BULK:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Comparisons of Smoke Components in the Semivolatile Phase from Lamina and Midrib Cigarettes of Flue-cured Tobacco Leaves.
Ishiguro S and Sugawara S.
Agricultural and Biological Chemistry, 42(8), 1527-1531 (1978)
2, 5-Dimethylphenacyl as a new photoreleasable protecting group for carboxylic acids.
Klan P, et al.
Organic Letters, 2(11), 1569-1571 (2000)
A laser flash photolysis study of the mechanism of the photocyclization of. alpha.-chloro-ortho-methylacetophenones.
Netto-Ferreira JC and Scaiano JC.
Journal of the American Chemical Society, 113(15), 5800-5803 (1991)
Rapid Photochemical Synthesis of 6-Methyl-1-Indanone.
Wang S, et al.
Advanced Materials Research, 634-638, 416-419 (2013)
Andrew M Booth et al.
Environmental science & technology, 42(21), 8122-8126 (2008-11-27)
Previously, comprehensive two-dimensional gas chromatography-time of flight-mass-spectrometry (GCxGC-ToF-MS) revealed that the unresolved complex mixtures (UCMs) of contaminant hydrocarbons accumulated by health-affected mussels Mytilus edulis (up to 125 microg g dry weight(-1)) collected from around U.K. coasts, included many isomeric branched

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